Omegia Softgel Clinical Research Program

Chia Nan University of Pharmacy ＆ Science40 enrolled

Overview

Evaluate the improvement of regulation of skin and blood index composition after consumption of Omegia® Softgel

The blood biochemical analysis at Weeks 0 and 12, including Catalase, Tumor necrosis factor-α, Cholesterol, Triglyceride, High-density lipoprotein-Cholesterol and Low-density lipoprotein- Cholesterol. The Skin assessment at Weeks 0, 4 and 12, including Skin brightness, Skin redness sensitivity index, Skin moisture, Skin elasticity, Facial skin pores, Facial skin texture and Skin collagen content.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

SUPPORTIVE_CARE

Masking

TRIPLE

Enrollment

Conditions

Skin Manifestations Antioxidative Stress Eye Strain Vaginal Disease

Interventions

Omegia® Softgel -BDIETARY_SUPPLEMENT

How to use: Take once a day for 12 weeks Subject precautions: If the health products and cosmetic care products used contain sea buckthorn ingredients, stop using them.

Omegia® Softgel -ADIETARY_SUPPLEMENT

How to use: Take once a day for 12 weeks Subject precautions: If the health products and cosmetic care products used contain sea buckthorn ingredients, stop using them.

Eligibility

Sex: FEMALEMin age: 45 YearsMax age: 75 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: ● Female subjects older than 45 years Exclusion Criteria: * Involuntary subjects * Skin disease, liver cirrhosis or chronic renal failure * Those with known cosmetic, drug or food allergies * Pregnant women and nursing mothers. * Those taking chronic disease medication * The subject has received laser facial treatment, fruit acid facial peeling, long-term sunlight, etc. within four weeks of the test

Locations (1)

Chia Nan University of Pharmacy ＆ Science

Tainan, Taiwan

Outcomes

Primary Outcomes

Skin brightness

Skin color difference analyzer (Chroma Meter MM500) was utilized to measure skin brightness. Units: arbitrary units